FDA Drug Recalls

Recalls / Class II

Class IID-0275-2020

Product

S-MIC 25/50/50MG/ML B12A1MG/ML MDV INJ SOLN; Rx Only, a) 10ML b) 30ML glass vial. Red Mountain Compounding RX.

Affected lot / code info
Lot #: a) S03272019DT@04, Exp 09/27/2019, b) S01302019DT@08, Exp 08/30/2019, S02192019DH@10, Exp 08/19/2019, S03072019DH@01, Exp 09/07/2019, S03042019DH@02, Exp 09/07/2019, S03272019DT@04, Exp 09/27/2019, S04172019DT@03, Exp 10/17/2019, S04302019DT@11, Exp 10/30/2019, S05162019DH@20, Exp 11/16/2019, S05292019DT@03, Exp 11/29/2019, S06252019DH@17, Exp 12/25/2019, S07172019DT@12, Exp 01/17/2020, S07182019DT@08, Exp 01/18/2020,

Why it was recalled

Lack of Assurance of Sterility

Recalling firm

Firm
First Royal Care Co. LLC, dba Red Mountain Compounding Pharmacy
Notification channel
Letter
Type
Voluntary: Firm initiated
Address
6828 E Brown Rd Ste 101, N/A, Mesa, Arizona 85207-3761

Distribution

Quantity
108x 10 and 30 ml glass vials
Distribution pattern
Nationwide in the USA

Timeline

Recall initiated
2019-08-12
FDA classified
2019-11-05
Posted by FDA
2019-11-13
Terminated
2023-04-13
Status
Terminated

Source: openFDA Drug Enforcement endpoint. Recall record D-0275-2020. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.

Class II recall: drug · FDA Drug Recalls